A seawater desalination scheme for global hydrological models

Seawater desalination is a practical technology for providing fresh water to coastal arid regions. Indeed, the use of desalination is rapidly increasing due to growing water demand in these areas and decreases in production costs due to technological advances. In this study, we developed a model to estimate the areas where seawater desalination is likely to be used as a major water source and the likely volume of production. The model was designed to be incorporated into global hydrological models (GHMs) that explicitly include human water usage. The model requires spatially detailed information on climate, income levels, and industrial and municipal water use, which represent standard input/output data in GHMs. The model was applied to a specific historical year (2005) and showed fairly good reproduction of the present geographical distribution and national production of desalinated water in the world. The model was applied globally to two periods in the future (2011-2040 and 2041-2070) under three distinct socioeconomic conditions, i.e., SSP (shared socioeconomic pathway) 1, SSP2, and SSP3. The results indicate that the usage of seawater desalination will have expanded considerably in geographical extent, and that production will have increased by 1.4-2.1-fold in 2011-2040 compared to the present (from 2.8×109 m3 yr-1 in 2005 to 4.0-6.0×109 m3 yr-1/, and 6.7-17.3-fold in 2041-2070 (from 18.7 to 48.6×109 m3 yr-1/. The estimated global costs for production for each period are USD 1.1-10.6×109 (0.002-0.019% of the total global GDP), USD 1.6-22.8×109 (0.001-0.020 %), and USD 7.5-183.9×109 (0.002-0.100 %), respectively. The large spreads in these projections are primarily attributable to variations within the socioeconomic scenarios

Induction of Non-Targeted Stress Responses in Mammary Tissues by Heavy Ions

Purpose Side effects related to radiation exposures are based primarily on the assumption that the detrimental effects of radiation occur in directly irradiated cells. However, several studies have reported over the years of radiation-induced non-targeted/ abscopal effects in vivo that challenge this paradigm. There is evidence that Cyclooxygenase-2 (COX2) plays an important role in modulating non-targeted effects, including DNA damages in vitro and mutagenesis in vivo. While most reports on radiation-induced non-targeted response utilize x-rays, there is little information available for heavy ions. Methods and Materials Adult female transgenic gpt delta mice were exposed to an equitoxic dose of either carbon or argon particles using the Heavy Ion Medical Accelerator in Chiba (HIMAC) at the National Institute of Radiological Sciences (NIRS) in Japan. The mice were stratified into 4 groups of 5 animals each: Control; animals irradiated under full shielding (Sham-irradiated); animals receiving whole body irradiation (WBIR); and animals receiving partial body irradiation (PBIR) to the lower abdomen with a 1 x 1 cm2 field. The doses used in the carbon ion group (4.5 Gy) and in argon particle group (1.5 Gy) have a relative biological effectiveness equivalent to a 5 Gy dose of x-rays. 24 hours after irradiation, breast tissues in and out of the irradiated field were harvested for analysis. Induction of COX2, 8-hydroxydeoxyguanosine (8-OHdG), phosphorylated histone H2AX (γ-H2AX), and apoptosis-related cysteine protease-3 (Caspase-3) antibodies were examined in the four categories of breast tissues using immunohistochemical techniques. Analysis was performed by measuring the intensity of more than 20 individual microscopic fields and comparing the relative fold difference. Results In the carbon ion group, the relative fold increase in COX2 expression was 1.01 in sham-irradiated group (p > 0.05), 3.07 in PBIR (p 0.05), 11.31 in PBIR (p 0.05), 8.41 in PBIR (p < 0.05) and 10.59 in WBIR (p < 0.05). Results for the argon particle therapy group showed a similar magnitude of changes in the various biological endpoints examined. There was no statistical significance observed in Caspase-3 expression among the 4 groups. Conclusions Our data show that both carbon and argon ions induced non-targeted, out of field induction of COX2 and DNA damages in breast tissues. These effects may pose new challenges to evaluate the risks associated with radiation exposure and understanding radiation-induced side effects

Emergence of Clostridium botulinum type B-like nontoxigenic organisms in a patient with type B infant botulism

金沢大学大学院医学系研究科病態検査学We encountered a patient with infant botulism caused by a single clone of Clostridium botulinum type B. In the early convalescent phase, a C. botulinum type B-like nontoxigenic organism emerged in the feces instead. Growth inhibition of toxigenic strains by nontoxigenic strains was examined

CXCR2 deficient mice display macrophage-dependent exaggerated acute inflammatory responses

CXCR2 is an essential regulator of neutrophil recruitment to inflamed and damaged sites and plays prominent roles in inflammatory pathologies and cancer. It has therefore been highlighted as an important therapeutic target. However the success of the therapeutic targeting of CXCR2 is threatened by our relative lack of knowledge of its precise in vivo mode of action. Here we demonstrate that CXCR2-deficient mice display a counterintuitive transient exaggerated inflammatory response to cutaneous and peritoneal inflammatory stimuli. In both situations, this is associated with reduced expression of cytokines associated with the resolution of the inflammatory response and an increase in macrophage accumulation at inflamed sites. Analysis using neutrophil depletion strategies indicates that this is a consequence of impaired recruitment of a non-neutrophilic CXCR2 positive leukocyte population. We suggest that these cells may be myeloid derived suppressor cells. Our data therefore reveal novel and previously unanticipated roles for CXCR2 in the orchestration of the inflammatory response